Coated shaped metal material

ABSTRACT

The present invention relates to a coated shaped metal material that is excellent in adhesion to a molded article of a thermoplastic resin composition and can be easily produced. The coated shaped metal material comprises a shaped metal material and a coating formed on a surface of the shaped metal material. The shaped metal material is a product made of a metal and has a predetermined shape by applying heat or force to the metal. The coating comprises a polyurethane resin containing a polycarbonate unit. A mass ratio of the polycarbonate unit to a total resin mass in the coating is 15 to 80 mass %. The coating has a film thickness of 0.5 to 20 μm.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.14/389,197, filed on Sep. 29, 2014, which is National Stage Applicationof International Application No. PCT/JP2013/002039, filed on Mar. 26,2013, the disclosure of which, including the specification, drawings andabstract, is incorporated herein by reference in their entirety.International Application No. PCT/JP2013/002039 is entitled to andclaims the benefit of Japanese Patent Application No. 2012-079751, filedon Mar. 30, 2012, and Japanese Patent Application No. 2012-246469, filedon Nov. 8, 2012, the disclosures of which, including the specifications,drawings and abstracts, are incorporated herein by reference in theirentirety.

TECHNICAL FIELD

The present invention relates to a coated shaped metal material, acomposite including a molded article of a thermoplastic resincomposition joined to the coated shaped metal material, and a method forproducing the composite.

BACKGROUND OF THE INVENTION

So-called “shaped metal materials” are used in various industrialproducts such as automobiles. The term “shaped metal material” usedherein refers to a product made of a metal given some shape by theapplication of heat, force, or the like. Examples of the shaped metalmaterials include metal sheets, press-molded products of metal sheets,and metal members shaped by processing methods such as casting, forging,cutting, and powder metallurgy. A composite including a molded articleof a resin composition joined to such a shaped metal material is used invarious electronic devices such as cellular mobile phones and personalcomputers, because the composite is lighter than a part made only of ametal and is stronger than a part made only of a resin. Such a compositehas heretofore been produced by the fitting together the shaped metalmaterial and the molded article of a resin composition. This method forproducing the composite by fitting, however, requires a large number ofsteps of operation and has low productivity. Accordingly, in recentyears, the composite has generally been produced by joining the moldedarticle of a resin composition to the shaped metal material by means ofinsert molding.

For the production of the composite by insert molding, it is importantto improve the adhesion between the shaped metal material and the moldedarticle of a resin composition. For example, the roughening treatment ofthe surface of the shaped metal material prior to insert molding hasbeen proposed as a method for enhancing the adhesion between the shapedmetal material and the molded article of a resin composition (see PTLs 1to 3). The methods disclosed in PTLs 1 to 3 involve roughening thesurface of an aluminum alloy to thereby improve the joinability of thealuminum alloy to a molded article of a resin composition.

CITATION LIST Patent Literature PTL 1 Japanese Patent ApplicationLaid-Open No. 2006-027018 PTL 2 Japanese Patent Application Laid-OpenNo. 2004-050488 PTL 3 Japanese Patent Application Laid-Open No.2005-342895 SUMMARY OF INVENTION Technical Problem

The composites described in PTLs 1 to 3 produce undesired insufficientadhesion between the shaped metal material and the molded article of aresin composition due to joining based on an anchor effect. In addition,the methods for producing the composites described in PTLs 1 to 3unfavorably have complicated production steps and increased productioncost due to the roughening treatment of the surface of the shaped metalmaterial.

An object of the present invention is to provide a coated shaped metalmaterial that is excellent in adhesion to a molded article of athermoplastic resin composition and can be easily produced.

Solution to Problem

The present inventors have found that the above-mentioned problems canbe solved by forming a predetermined coating on the surface of a shapedmetal material. The present inventors have further conducted studies andthereby completed the present invention.

Specifically, the present invention relates to the following coatedshaped metal materials:

[1] A coated shaped metal material including: a shaped metal material;and a coating formed on the surface of the shaped metal material, theshaped metal material being a product made of a metal and having apredetermined shape by applying heat or force to the metal, the coatingincluding a polyurethane resin containing a polycarbonate unit, in whichthe mass ratio of the polycarbonate unit to the total resin mass in thecoating is 15 to 80 mass %, and the coating has a film thickness of 0.5to 20 μm.

[2] The coated shaped metal material according to [1], in which thecoating includes an oxide, a hydroxide, or a fluoride of a metalselected from the group consisting of Ti, Zr, V, Mo, and W, or acombination thereof.

Advantageous Effects of Invention

The present invention can provide a coated shaped metal material that isexcellent in adhesion to a molded article of a thermoplastic resincomposition and can be easily produced.

DESCRIPTION OF EMBODIMENTS

1. Coated Shaped Metal Material

The coated shaped metal material of the present invention includes: ashaped metal material; and a coating formed on the surface of the shapedmetal material. The coated shaped metal material may also have achemical conversion film formed between the shaped metal material andthe coating. Hereinafter, each component of the coated shaped metalmaterial will be described.

(1) Shaped Metal Material

The shaped metal material serving as a base material to be coated is notparticularly limited by its type. Examples of the shaped metal materialinclude: metal sheets such as cold-rolled steel sheets, zinc-coatedsteel sheets, Zn—Al alloy-coated steel sheets, Zn—Al—Mg alloy-coatedsteel sheets, Zn—Al—Mg—Si alloy-coated steel sheets, aluminum-coatedsteel sheets, stainless steel sheets (including austenitic, martensitic,ferritic, and ferrite-martensite duplex-phase stainless steel sheets),aluminum sheets, aluminum alloy sheets, and copper sheets; pressedproducts of metal sheets; and various metal members shaped by processingmethods such as casting (aluminum die-casting, zinc die-casting, etc.),forging, cutting, and powder metallurgy. The shaped metal material maybe subjected, if necessary, to coating pretreatment known in the artsuch as degreasing or pickling.

(2) Chemical Conversion Film As mentioned above, the coated shaped metalmaterial may also have a chemical conversion film formed between theshaped metal material and the coating. The chemical conversion film isformed on the surface of the shaped metal material and improves theadhesion of the coating to the shaped metal material and the corrosionresistance of the shaped metal material. The chemical conversion filmmay be formed on at least a region (junction surface) to be joined witha molded article of a thermoplastic resin composition mentioned later,of the surface of the shaped metal material, and is usually formed onthe whole surface of the shaped metal material.

The chemical conversion treatment to form the chemical conversion filmis not particularly limited by its type. Examples of the chemicalconversion treatment include chromate conversion treatment,chromium-free conversion treatment, and bonderizing treatment. Thechemical conversion film formed by the chemical conversion treatment isnot particularly limited by its coverage as long as the coverage fallswithin a range effective for improving the coating adhesion and thecorrosion resistance. For example, the coverage of the chromate film canbe adjusted such that the coverage attains 5 to 100 mg/m² in terms ofthe total amount of Cr. The coverage of the chromium-free film can beadjusted such that the coverage of a Ti—Mo composite film falls within arange of 10 to 500 mg/m² or the coverage of a fluoro acid film fallswithin a range of 3 to 100 mg/m² in terms of the amount of fluorine orin terms of the total amount of metal elements. The coverage of thephosphate film can be adjusted to 0.1 to 5 g/m².

(3) Coating

The coating includes a polyurethane resin containing a polycarbonateunit and improves the adhesion of a molded article of a thermoplasticresin composition to the shaped metal material. As mentioned later, thecoating may further contain a polycarbonate unit-free resin as anoptional component. The coating, as with the chemical conversion film,may be formed on at least the junction surface of the surface of theshaped metal material and is usually formed on the whole surface of theshaped metal material (or the chemical conversion film).

The polyurethane resin containing a polycarbonate unit has apolycarbonate unit in its molecular chain. The “polycarbonate unit”refers to a structure shown below in the molecular chain of thepolyurethane resin. The polyurethane resin containing a polycarbonateunit is similar in backbone (such as a benzene ring) and functionalgroup to a thermoplastic resin contained in a molded article of athermoplastic resin composition mentioned later. Accordingly, in thecase of insert-molding the thermoplastic resin composition to the coatedshaped metal material, the polyurethane resin containing a polycarbonateunit is uniformly blended with the thermoplastic resin composition toform a strong bond therebetween. Thus, the polyurethane resin containinga polycarbonate unit, contained in the coating, can improve the adhesionof a molded article of the thermoplastic resin composition to thecoating.

The polyurethane resin containing a polycarbonate unit can be prepared,for example, by steps described below. An organic polyisocyanate isreacted with a polycarbonate polyol and a polyol having a tertiary aminogroup or a carboxyl group to form a urethane prepolymer. Polyols otherthan the polycarbonate polyol compound, for example, polyester polyoland polyether polyol, may be used in combination to a extent that doesnot compromise the objects of the present invention.

The tertiary amino group of the urethane prepolymer thus produced can beneutralized with an acid or quaternized with a quaternizing agent,followed by chain elongation using water to form a cationic polyurethaneresin containing a polycarbonate unit.

Alternatively, the carboxyl group of the produced urethane prepolymercan be neutralized with a basic compound such as triethylamine,trimethylamine, diethanolmonomethylamine, diethylethanolamine, causticsoda, or caustic potassium for conversion to a carboxylate to form ananionic polyurethane resin containing a polycarbonate unit.

The polycarbonate polyol is obtained through the reaction of a carbonatecompound such as dimethyl carbonate, diethyl carbonate, ethylenecarbonate, or propylene carbonate with a diol compound such as ethyleneglycol, propylene glycol, dipropylene glycol, neopentyl glycol,methylpentanediol, dimethylbutanediol, butyl ethyl propanediol,diethylene glycol, triethylene glycol, tetraethylene glycol,1,4-butanediol, 1,4-cyclohexanediol, or 1,6-hexanediol. Thepolycarbonate polyol may be obtained by chain elongation from anisocyanate compound.

The organic polyisocyanate is not particularly limited by its type.Examples of the organic polyisocyanate include 2,4-tolylenediisocyanate, 2,6-tolylene diisocyanate, m-phenylene diisocyanate,p-phenylene diisocyanate, 4,4′-diphenylmethane diisocyanate,2,4′-diphenylmethane diisocyanate, 2,2′-diphenylmethane diisocyanate,3,3′-dimethyl-4,4′-biphenylene diisocyanate,3,3′-dichloro-4,4′-biphenylene diisocyanate, 1,5-naphthalenediisocyanate, 1,5-tetrahydronaphthalene diisocyanate, tetramethylenediisocyanate, 1,6-hexamethylene diisocyanate, dodecamethylenediisocyanate, trimethylhexamethylene diisocyanate, 1,3-cyclohexylenediisocyanate, 1,4-cyclohexylene diisocyanate, xylylene diisocyanate,tetramethylxylylene diisocyanate, hydrogenated xylylene diisocyanate,lysine diisocyanate, isophorone diisocyanate, and4,4′-dicyclohexylmethane diisocyanate. These organic polyisocyanates maybe used alone or in combination.

The coating may further contain a polycarbonate unit-free resin as anoptional component. The polycarbonate unit-free resin further improvesthe adhesion of the coating to the shaped metal material. Thepolycarbonate unit-free resin is not particularly limited by its type aslong as the resin contains no polycarbonate unit in its molecular chain.A polycarbonate unit-free resin containing a polar group is preferredfrom the viewpoint of improving the adhesion of the coating to theshaped metal material. Examples of the type of the polycarbonateunit-free resin include epoxy resins, polyolefin resins, phenol resins,acrylic resins, polyester resins, and polycarbonate unit-freepolyurethane resins. These resins may be used alone or in combination.

Examples of the epoxy resins include bisphenol A epoxy resins, bisphenolF epoxy resins, and bisphenol AD epoxy resins. Examples of thepolyolefin resins include polyethylene resins and polypropylene resins.Examples of the phenol resins include novolac resins and resol resins.The polycarbonate unit-free polyurethane resins are obtained by thecopolymerization of diols and diisocyanates. Examples of the diolsinclude diols other than polycarbonate diol, for example, bisphenol A,1,6-hexanediol, and 1,5-pentanediol. Examples of the diisocyanatesinclude aromatic diisocyanates, aliphatic diisocyanates, and alicyclicdiisocyanates.

The mass ratio of the polycarbonate unit to the total resin mass is 15to 80 mass %. A polycarbonate unit at a mass ratio less than 15 mass %might insufficiently produce the adhesion of a molded article of athermoplastic resin composition to the coating. On the other hand, apolycarbonate unit at a mass ratio exceeding 80 mass % mightinsufficiently produce the adhesion of the coating to the shaped metalmaterial. The mass ratio of the polycarbonate unit to the total resinmass can be determined by nuclear magnetic resonance spectroscopy (NMRanalysis) using a sample of the coating dissolved in chloroform.

Preferably, the coating further contains an oxide, a hydroxide, or afluoride of a metal (valve metal) selected from the group consisting ofTi, Zr, V, Mo, and W, or a combination thereof. Any of these metalcompounds dispersed in the coating can further improve the corrosionresistance of the shaped metal material. Particularly, the fluorides ofthese metals can also be expected to suppress the corrosion of a filmdefect area by virtue of their self-repairing effects.

The coating may further contain a soluble or poorly soluble metalphosphate or complex phosphate. The soluble metal phosphate or complexphosphate further improves the corrosion resistance of the shaped metalmaterial by complementing the self-repairing effects of the metalfluoride(s) mentioned above. The poorly soluble metal phosphate orcomplex phosphate dispersed in the coating improves film strength. Thesoluble or poorly soluble metal phosphate or complex phosphate is, forexample, a salt of Al, Ti, Zr, Hf, Zn, or the like.

The coating is not particularly limited by its film thickness as long asthe film thickness is 0.5 μm or larger. A coating having a filmthickness smaller than 0.5 μm might not be able to sufficiently improvethe adhesion of a molded article of a thermoplastic resin composition tothe shaped metal material. The upper limit of the film thickness of thecoating is not particularly limited and may be approximately 20 μm. Thecoating, even if having a film thickness exceeding 20 μm, cannot beexpected to further improve the adhesion.

The coating may be supplemented with an etching agent, an inorganiccompound, a lubricant, a color pigment, a dye, and the like in additionto the resin(s) mentioned above. The etching agent improves the adhesionof the coating to the shaped metal material by activating the surface ofthe shaped metal material. A fluoride such as hydrofluoric acid,ammonium fluoride, fluorozirconic acid, or fluorotitanic acid is used asthe etching agent. The inorganic compound improves water resistance bydensifying the coating. Examples of the inorganic compound include: solsof inorganic oxides such as silica, alumina, and zirconia; andphosphates such as sodium phosphate, calcium phosphate, manganesephosphate, and magnesium phosphate. Examples of the lubricant include:organic lubricants such as fluorine-based lubricants, polyethylene-basedlubricants, and styrene-based lubricants; and inorganic lubricants suchas molybdenum disulfide and talc. Further addition of an inorganicpigment, an organic pigment, an organic dye, or the like may impart apredetermined color tone to the coating.

The coated shaped metal material of the present invention is notparticularly limited by its production method. The coated shaped metalmaterial of the present invention can be produced, for example, by thefollowing method.

First, the shaped metal material serving as a base material to be coatedis provided. When the chemical conversion film is formed, chemicalconversion treatment is performed prior to formation of the coating.When the chemical conversion film is not formed, the coating is formeddirectly thereon.

In the case of forming the chemical conversion film on the surface ofthe shaped metal material, the chemical conversion film can be formed bythe application of a chemical conversion treatment solution to thesurface of the shaped metal material followed by drying. The method forapplying the chemical conversion treatment solution is not particularlylimited and can be appropriately selected from methods known in the art.Examples of such application methods include roll coating, curtain flow,spin coating, spraying, and dip-drawing methods. The conditions for thedrying of the chemical conversion treatment solution may beappropriately set according to the composition of the chemicalconversion treatment solution, etc. For example, the shaped metalmaterial having the chemical conversion treatment solution appliedthereon can be placed in a drying oven without being washed with water,and then heated at a peak plate temperature within a range of 80 to 250°C. to form a uniform chemical conversion film on the surface of theshaped metal material.

The coating can be formed on the surface of the shaped metal material(or the chemical conversion film) by the application thereto of acoating material containing the above-mentioned polyurethane resincontaining a polycarbonate unit followed by baking. The method forapplying the coating material is not particularly limited and can beappropriately selected from methods known in the art. Examples of suchapplication methods include roll coating, curtain flow, spin coating,spraying, and dip-drawing methods. The conditions for the baking of thecoating material may be appropriately set according to the compositionof the coating material, etc. For example, the shaped metal materialhaving the coating material applied thereon can be placed in a dryingoven and dried with a hot-air dryer at a peak plate temperature within arange of 110 to 200° C. to form a uniform coating on the surface of theshaped metal material (or the chemical conversion film).

As described above, the coated shaped metal material of the presentinvention has the coating containing a predetermined amount of thepolyurethane resin containing a polycarbonate unit and is thereforeexcellent in adhesion to a molded article of a thermoplastic resincomposition. In addition, the coated shaped metal material of thepresent invention can be easily produced merely by the application ofthe coating material containing the polyurethane resin containing apolycarbonate unit followed by baking.

2. Composite

A molded article of a thermoplastic resin composition can be joined tothe surface of the coated shaped metal material of the present inventionto produce a composite.

The molded article of a thermoplastic resin composition is joined to thesurface of the above-mentioned coated shaped metal material (moreaccurately, the surface of the coating). The shape of the molded articleof a thermoplastic resin composition is not particularly limited and canbe appropriately selected according to use.

The thermoplastic resin constituting the molded article of athermoplastic resin composition is not particularly limited by its type.Examples of the thermoplastic resin includeacrylonitrile-butadiene-styrene (ABS) resins, polyethylene terephthalate(PET) resins, polybutylene terephthalate (PBT) resins, polycarbonate(PC) resins, polyamide (PA) resins, and polyphenylene sulfide (PPS)resins, and combinations thereof. Among them, a thermoplastic resincontaining a benzene ring, as with the polycarbonate unit, is preferred,and a PBT resin or a PPS resin is particularly preferred.

The PBT resin is obtained, for example, by the condensation of1,4-butanediol with terephthalic acid and has the following structure:

The PPS resin is obtained, for example, by the condensation ofp-dichlorobenzene with sodium sulfide in an amide solvent and has thefollowing structure:

The thermoplastic resin composition may also contain an inorganicfiller, a thermoplastic polymer, and the like, from the viewpoint ofmold shrinkage factors, material strength, mechanical strength, scratchresistance, etc. Particularly, for using the thermoplastic resin havingno benzene ring, it is preferred to add thereto a thermoplastic polymerhaving a benzene ring.

The inorganic filler improves the rigidity of the molded article of thethermoplastic resin composition. The inorganic filler is notparticularly limited by its type, and a known substance can be used.Examples of the inorganic filler include: fibrous fillers such as glassfibers, carbon fibers, and aramid resins; powder fillers such as carbonblack, calcium carbonate, calcium silicate, magnesium carbonate, silica,talc, glass, clay, lignin, mica, quartz powders, and glass spheres; andpulverized carbon fibers or aramid fibers. The content of the inorganicfiller is not particularly limited and is preferably within a range of 5to 50 mass %. These inorganic fillers may be used alone or incombination.

The thermoplastic polymer improves the shock resistance of the moldedarticle of the thermoplastic resin composition. The thermoplasticpolymer is not particularly limited by its type. Examples of thethermoplastic polymer having a benzene ring includeacrylonitrile-butadiene-styrene resins, polyethylene terephthalateresins, polybutylene terephthalate resins, polycarbonate resins,polystyrene resins, and polyphenylene ether resins. Examples of thethermoplastic polymer having no benzene ring include polyolefin resins.These thermoplastic polymers may be used alone or in combination.

3. Method for Producing Composite

A method for producing the composite of the present inventionincludes: 1) providing a coated shaped metal material; 2) inserting thecoated shaped metal material into an injection molding die; and 3)joining a molded article of a thermoplastic resin composition to thesurface of the coated shaped metal material.

Hereinafter, these procedures of the present invention will bedescribed.

Step (1)

A coated shaped metal material is provided by the procedures mentionedabove.

Step (2)

The coated shaped metal material thus provided is inserted into aninjection molding die. The coated shaped metal material may be processedinto a desired shape by pressing or the like.

Step (3)

A thermoplastic resin composition having a high temperature is injectedat a high pressure into the injection molding die having the coatedshaped metal material thus inserted therein. In this respect, theinjection molding die is preferably provided with a degassing port thatallows the thermoplastic resin composition to flow smoothly. Thethermoplastic resin composition having a high temperature comes incontact with the coating formed on the surface of the coated shapedmetal material. The temperature of the injection molding die ispreferably around the melting point of the thermoplastic resincomposition.

After the completion of the injection, the die is opened and released toobtain a composite. The composite obtained by injection molding may besubjected to annealing treatment after the molding to cancel internalstrain ascribable to mold shrinkage.

The composite of the present invention can be produced by theseprocedures.

As described above, a molded article of a thermoplastic resincomposition can be joined to the surface of the coated shaped metalmaterial of the present invention to produce a composite. The coatedshaped metal material of the present invention has a predeterminedcoating that is excellent in adhesion both to the shaped metal materialand to the molded article of a thermoplastic resin composition. For thisreason, the composite of the present invention is excellent in theadhesion between the shaped metal material and the molded article of athermoplastic resin composition.

Hereinafter, the present invention will be described in detail withreference to Examples. However, the present invention is not intended tobe limited by these Examples.

EXAMPLES Example 1

In Example 1, each coated shaped metal material was provided andexamined for its corrosion resistance.

1. Preparation of Coated Shaped Metal Material

(1) Shaped Metal Material

Stainless steel sheets, a molten Zn—Al—Mg alloy-coated steel sheet, amolten Al-coated steel sheet, and molten Al-containing Zn-coated steelsheets were provided as base materials to be coated for coated shapedmetal materials.

A. Stainless Steel Sheet

SUS304 and SUS430 (both 2D-finish) having a sheet thickness of 0.8 mmwere provided as stainless steel sheets.

B. Molten Zn—Al—Mg Alloy-Coated Steel Sheet

A molten Zn-6 mass % Al-3 mass % Mg alloy-coated steel sheet having acoating coverage of 45 g/m² on one side was provided as a moltenZn—Al—Mg alloy-coated steel sheet. The base steel sheet used was acold-rolled steel sheet (SPCC) having a sheet thickness of 0.8 mm.

C. Molten Al-Coated Steel Sheet

A molten Al-9 mass % Si alloy-coated steel sheet having a coatingcoverage of 45 g/m² on one side was provided as a molten Al-coated steelsheet. The base steel sheet used was a cold-rolled steel sheet (SPCC)having a sheet thickness of 0.8 mm.

D. Molten Al-Containing Zn-Coated Steel Sheet

A molten Zn-0.18 mass % Al alloy-coated steel sheet and a molten Zn-55mass % Al alloy-coated steel sheet each having a coating coverage of 45g/m² on one side were provided as molten Al-containing Zn-coated steelsheets. Both of the base steel sheets used were cold-rolled steel sheets(SPCC) having a sheet thickness of 0.8 mm.

(2) Preparation of Coating Material

Each polycarbonate unit-containing resin, each polycarbonate unit-freeresin, and various additives were added to water such that the massratio of the polycarbonate (PC) unit to the total resin mass attainedthe predetermined ratio shown in Table 1 to prepare a coating materialhaving 20% nonvolatile components (see Table 1). When a plurality ofpolycarbonate unit-free resins were used, these polycarbonate unit-freeresins were added thereto in equal amounts. Each coating material wassupplemented with 0.5 mass % of ammonium fluoride (Morita ChemicalIndustries Co., Ltd.) as an etching agent, 2 mass % of colloidal silica(Nissan Chemical Industries, Ltd.) as an inorganic compound, and 0.5mass % of phosphoric acid (Kishida Chemical Co., Ltd.).

A. Polycarbonate Unit-Containing Resin

As for each polycarbonate unit-containing resin shown in Table 1, SF-420(Dai-Ichi Kogyo Seiyaku Co., Ltd.) was used as a polyurethane resincontaining 50 mass % of the polycarbonate unit. SF-470 (Dai-Ichi KogyoSeiyaku Co., Ltd.) was used as a polyurethane resin containing 70 mass %of the polycarbonate unit. HUX-386 (ADEKA Corp.) was used as apolyurethane resin containing 80 mass % of the polycarbonate unit. Aproduct under test provided by a resin manufacturer was used as apolyurethane resin containing 90 mass % of the polycarbonate unit. Aresin composition composed of 100 mass % of the polycarbonate unit wasprepared by the following method: a polycarbonate sheet (TAKIRON Co.,Ltd.) having a sheet thickness of 2.0 mm was cut into approximately 5 mmsquare to obtain polycarbonate pieces. To 200 g of methylene chloride,30 g of the polycarbonate pieces thus cut was added, and the mixture wasstirred for 3 hours under heating to a solution temperature of 40° C. todissolve the polycarbonate pieces in methylene chloride. The resincomposition composed of 100 mass % of the polycarbonate unit wasprepared by this step.

B. Polycarbonate Unit-Free Resin

As for each polycarbonate unit-free resin shown in Table 1, HUX-232(ADEKA Corp.) or SF-170 (Dai-Ichi Kogyo Seiyaku Co., Ltd.) was used as apolycarbonate unit-free polyurethane resin. ADEKA Resin EM-0461N (ADEKACorp.) or Super Ester E650 (Arakawa Chemical Industries, Ltd.) was usedas an epoxy resin. HARDLEN NZ-1005 (Toyobo Co., Ltd.) or MGP1650(Maruyoshi Chemical Co., Ltd.) was used as a polyolefin resin. TAMANOLE-100 (Arakawa Chemical Industries, Ltd.) or IG-1002 (DIC Corp.) wasused as a phenol resin.

(3) Formation of Coating

Each base material to be coated was dipped for 1 minute in an aqueousalkali solution for degreasing (pH=12) having a solution temperature of60° C. to degrease the surface. Subsequently, each coating material wasapplied to the degreased surface of the base material to be coated usinga roll coater and dried with a hot-air dryer at a peak metal temperatureof 150° C. to form a coating having the film thickness shown in Table 1.

TABLE 1 Film thickness Base Coated PC unit- of material shaped metal PCunit containing PC unit- coating to be material No. (mass %) resin freeresin (μm) coated 1 15 B a 1.0 1 2 15 B a, b 3.2 2 3 30 C b 0.5 3 4 30 Cb 1.6 4 5 30 C b, f 2.2 5 6 30 C b, c, f, h 3.0 6 7 30 C b, h 2.2 3 8 30D a 2.5 3 9 30 D a, d 1.1 3 10 30 D e, g 8.4 5 11 50 B a 4.1 1 12 50 C b3.3 4 13 70 B — 1.0 6 14 70 C a 1.0 3 15 80 C — 1.4 3 16 80 D b 1.8 3 1750 B a 0.4 5 18 80 D d 0.1 5 19 0 — a 2.3 2 20 0 — b, c 1.6 3 21 5 A a1.1 4 22 14 B a, e 3.5 5 23 85 D b 2.4 6 24 100 E — 0.8 3 —PCUnit-Containing Polyurethane Resin A: Polyurethane resin containing 50mass % of the PC unit (SF-420) B: Polyurethane resin containing 70 mass% of the PC unit (SF-470) C: Polyurethane resin containing 80 mass % ofthe PC unit (HUX-386) D: Polyurethane resin containing 90 mass % of thePC unit E: Resin composition composed of 100 mass % of the PC unit —PCUnit-Free Resin a: PC unit-free polyurethane resin (HUX-232) b: PCunit-free polyurethane resin (SF-170) c: Epoxy resin (ADEKA ResinEM-0461N) d: Epoxy resin (Super Ester E650) e: Polyolefin resin (HARDLENNZ-1005) f: Polyolefin resin (MGP1650) g: Phenol resin (TAMANOL E-100)h: Phenol resin (IG-1002) —Base Material to Be Coated 1: SUS304 2:SUS430 3: Molten Zn-6 mass % Al-3mass % Mg alloy-coated steel sheet 4:Molten Al-9 mass % Si alloy-coated steel sheet 5: Molten Zn-0.18 mass %Al alloy-coated steel sheet 6: Molten Zn-55 mass % Al alloy-coated steelsheet

2. Evaluation of Coated Shaped Metal Material

(1) Corrosion Resistance Test

A test piece (30 mm wide×100 mm long) was cut out of each coated shapedmetal material and subjected to the corrosion resistance test. Accordingto JIS Z 2371, an aqueous NaCl solution of 35° C. was sprayed onto eachtest piece with sealed end faces for 120 hours. After the spraying ofthe aqueous NaCl solution, each coated shaped metal material wasevaluated for its corrosion resistance on the basis of the occurrence ofwhite rust on the surface. The coated shaped metal material wasevaluated as “Poor” when the occurrence of white rust was 50 area % orlarger, as “Fair” when the occurrence of white rust was 20 area % orlarger and smaller than 50 area %, as “Good” when the occurrence ofwhite rust was 10 area % or larger and smaller than 20 area %, and as“Excellent” when the occurrence of white rust was smaller than 10 area%.

(2) Results

The occurrence of white rust on the provided coated shaped metalmaterials is shown in Table 2.

TABLE 2 Coated shaped Occurrence of metal material No. white rust (area%) 1  0 (Excellent) 2  0 (Excellent) 3  0 (Excellent) 4  0 (Excellent) 5 0 (Excellent) 6  0 (Excellent) 7  0 (Excellent) 8  0 (Excellent) 9  0(Excellent) 10  0 (Excellent) 11  0 (Excellent) 12  0 (Excellent) 13  0(Excellent) 14  0 (Excellent) 15  2 (Excellent) 16  2 (Excellent) 17  2(Excellent) 18  5 (Excellent) 19  0 (Excellent) 20  2 (Excellent) 21  0(Excellent) 22  3 (Excellent) 23  6 (Excellent) 24 12 (Good)

As shown in Table 2, all the provided coated shaped metal materials(coated shaped metal material Nos. 1 to 24) had favorable corrosionresistance. The roughened surface of a shaped metal material cannot besubjected to rust prevention treatment due to the need for exerting ananchor effect on a molded article of a thermoplastic resin composition.The resulting shaped metal material has poor corrosion resistance. Bycontrast, the coated shaped metal material used in the present inventionhas a resin coating formed on the surface of a base material to becoated and is therefore excellent in corrosion resistance.

Example 2

In Example 2, each composite of a coated shaped metal material and amolded article of a thermoplastic resin composition was prepared andexamined for the adhesion between the coated shaped metal material andthe molded article of a thermoplastic resin composition.

1. Preparation of Composite

(1) Coated Shaped Metal Material

Coated shaped metal material Nos. 1 to 24 of Example 1 were provided.

(2) Thermoplastic Resin Composition

Thermoplastic resin compositions shown in Table 3 were prepared. As foreach thermoplastic resin composition shown in Table 3, EXCELLOY CK10G20(no distinct melting point is confirmed; Techno Polymer Co., Ltd.) wasused as an acrylonitrile-butadiene-styrene (ABS) resin composition. Asample (melting point: 230° C.) provided by a resin manufacturer wasused as a polyethylene terephthalate (PET) resin composition. NOVADURAN5710F40 (melting point: 230° C.; Mitsubishi Engineering-Plastics Corp.)was used as a polybutylene terephthalate (PBT) resin composition.IUPILON GS-2030MR2 (melting point: 250° C.; MitsubishiEngineering-Plastics Corp.) was used as a polycarbonate (PC) resincomposition. Amilan CM3511G50 (melting point: 216° C.; Toray Industries,Inc.) was used as a polyamide (PA) resin composition. 1130MF1 (meltingpoint: 280° C.; Polyplastics Co., Ltd.) was used as a polyphenylenesulfide (PPS) resin composition. Each thermoplastic resin compositioncontained each filler shown in Table 3. The mold shrinkage factorrepresents a value measured in the flow direction.

TABLE 3 Thermoplastic Resin resin Mold temperature compositionThermoplastic Thermoplastic Filler shrinkage during injection No. resinpolymer (mass %) factor (%) molding (° C.) 1 ABS resin PC resin Glassfiber (20) 0.1 280 2 PET resin PC resin Glass fiber (30) 0.3 260 3 PBTresin PC resin Glass fiber (40) 0.3 260 4 PC resin — Glass fiber (30)0.2 310 5 PA resin Polyolefin resin Glass fiber (50) 0.2 280 6 PPS resinPolyolefin resin Glass fiber (40) 0.3 320

(3) Joining (Insert Molding) of Molded Article of Thermoplastic ResinComposition

Each coated shaped metal material was inserted into an injection moldingdie. Each thermoplastic resin composition in a molten state was injectedinto the injection molding die. The volume of a portion to which thethermoplastic resin composition is injected in the injection molding dieis 30 mm wide×100 mm long×4 mm thick. The coating is contacted with thethermoplastic resin composition in a region of 30 mm wide×30 mm long.The thermoplastic resin composition thus injected into the injectionmolding die was solidified to obtain a composite of the coated shapedmetal material and the molded article of the thermoplastic resin.

2. Evaluation of Adhesion

(1) Measurement of Peel Strength

The coated shaped metal material and the molded article of thethermoplastic resin composition were both pulled at a rate of 100 mm/minin the coplanar direction, and the strength at break (peel strength) wasmeasured. The composite was evaluated as “Poor” when the peel strengthwas less than 1.0 kN, as “Fair” when the peel strength was 1.0 kN ormore and less than 1.5 kN, as “Good” when the peel strength was 1.5 kNor more and less than 2.0 kN, and as “Excellent” when the peel strengthwas 2.0 kN or more.

(2) Results

The results of measuring the peel strength of the evaluated compositesare shown in Table 4.

TABLE 4 Film Coated shaped Thermoplastic thickness Peel metalcomposition PC unit of coating strength Category material No. No. (mass%) (μm) (kN) Example 1 1 1 15 1.0 1.5 (Good) Example 2 2 2 15 3.2 1.5(Good) Example 3 3 3 30 0.5 1.6 (Good) Example 4 4 4 30 1.6 2.0(Excellent) Example 5 5 5 30 2.2 2.2 (Excellent) Example 6 6 6 30 3.02.1 (Excellent) Example 7 7 1 30 2.2 1.8 (Good) Example 8 8 2 30 2.5 1.7(Good) Example 9 9 3 30 1.1 2.0 (Excellent) Example 10 10 4 30 8.4 1.6(Good) Example 11 11 5 50 4.1 1.6 (Good) Example 12 12 6 50 3.3 2.3(Excellent) Example 13 13 4 70 1.0 1.8 (Good) Example 14 14 5 70 1.0 1.6(Good) Example 15 15 6 80 1.4 2.0 (Excellent) Example 16 16 5 80 1.8 2.1(Excellent) Example 17 3 6 30 0.5 1.6 (Good) Example 18 6 3 30 3.0 2.0(Excellent) Example 19 9 1 30 1.1 1.7 (Good) Example 20 10 3 30 8.4 2.3(Excellent) Example 21 12 6 50 3.3 2.2 (Excellent) Example 22 13 6 701.0 1.8 (Good) Example 23 16 3 80 1.8 2.0 (Excellent) Comparative 17 350 0.4 1.4 (Fair) Example 1 Comparative 18 5 80 0.1 1.0 (Fair) Example 2Comparative 19 3 0 2.3 0.0 (Poor) Example 3 Comparative 20 4 0 1.6 0.0(Poor) Example 4 Comparative 21 5 5 1.1 0.6 (Poor) Example 5 Comparative22 4 14 3.5 1.3 (Fair) Example 6 Comparative 23 5 85 2.4 1.3 (Fair)Example 7 Comparative 24 6 100 0.8 0.0 (Poor) Example 8

The composites of Comparative Examples 1 and 2 had poor adhesion betweenthe coated shaped metal material and the molded article of thethermoplastic resin composition, because their coatings had a filmthickness smaller than 0.5 μm. The composites of Comparative Examples 3to 8 had poor adhesion between the coated shaped metal material and themolded article of the thermoplastic resin composition, because the massratio of the polycarbonate unit to the total resin mass in theircoatings did not fall within the predetermined range. By contrast, thecomposites of Examples 1 to 23 had excellent adhesion between the coatedshaped metal material and the molded article of the thermoplastic resincomposition because their coatings had a film thickness that fell withinthe predetermined range and because the mass ratio of the polycarbonateunit to the total resin mass in their coatings fell within thepredetermined range.

INDUSTRIAL APPLICABILITY

The composite of the present invention is excellent in the adhesionbetween the coated shaped metal material and the molded article of athermoplastic resin composition and as such, is preferably used in, forexample, various electronic devices, consumer electronics, medicalequipment, automobile bodies, car interior accessories, andconstructional materials.

What is claimed is:
 1. A coated shaped metal material comprising: ashaped metal material; and a coating formed on a surface of the shapedmetal material, wherein the shaped metal material is a product made of ametal and has a predetermined shape by applying heat or force to themetal, the coating comprises a polyurethane resin containing apolycarbonate unit, a mass ratio of the polycarbonate unit to a totalresin mass in the coating is 15 to 80 mass %, and the coating has a filmthickness of 0.5 to 20 μm.
 2. The coated shaped metal material accordingto claim 1, wherein the coating comprises an oxide, a hydroxide, or afluoride of a metal selected from the group consisting of Ti, Zr, V, Mo,and W, or a combination thereof.